Sr. Process Engineer – Medical Device Manufacturing

Grove Technical Resources

Brooklyn Center (MN)

On-site

USD 90,000 - 120,000

Full time

11 days ago

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Job summary

Grove Technical Resources seeks a Sr. Process Engineer to support advanced manufacturing and welding process development for medical devices. The role emphasizes developing, qualifying, and optimizing joining processes to meet regulatory standards.

You will lead validations, data analysis, and cross‑functional collaboration with Quality, Operations, and R&D teams, contributing to cost‑reduction initiatives and successful product transfers.

Qualifications

  • Bachelor’s Degree in Engineering or related Science field.
  • 5+ years of Process/Manufacturing Engineering experience.
  • Hands-on experience with laser welding, resistance welding, battery/capacitor manufacturing, or related thermal joining technologies.

Responsibilities

  • Develop, optimize, and qualify welding/joining manufacturing processes
  • Execute process validations, data analysis, and technical documentation
  • Lead process improvement and cost‑reduction initiatives
  • Support new product introductions and transfer processes into production
  • Investigate process issues and drive corrective actions

Skills

Process Development
Validation
DOE
Root Cause Analysis
DMAIC
Statistical Analysis
Laser Welding
Resistance Welding
Micro-Welding
Medical Device Experience
IQ/OQ/PQ
CAPA
Minitab
SPC
Cross‑Functional Collaboration

Education

Bachelor's Degree in Engineering

Tools

Minitab

Job description

Hiring: Sr. Process Engineer – Medical Device Manufacturing
Type: W2 contract
Duration: 12+ Month Contract

We are seeking an experienced Sr. Process Engineer to support advanced manufacturing and welding process development for medical devices.

Key Skills Required:
  • Process Development, Validation, and Continuous Improvement
  • DOE (Design of Experiments), Root Cause Analysis, DMAIC, and Statistical Analysis
  • Laser Welding, Resistance Welding, Micro-Welding, or Similar Joining Processes
  • Medical Device or Other Highly Regulated Industry Experience
  • Process Qualification (IQ/OQ/PQ), CAPA, and Engineering Documentation
  • Minitab, SPC, and Manufacturing Process Optimization
  • Cross‑Functional Collaboration with Quality, Operations, and R&D Teams
Responsibilities:
  • Develop, optimize, and qualify welding/joining manufacturing processes
  • Execute process validations, data analysis, and technical documentation
  • Lead process improvement and cost‑reduction initiatives
  • Support new product introductions and transfer processes into production
  • Investigate process issues and drive corrective actions
Requirements:
  • Bachelor’s Degree in Engineering or related Science field
  • 5+ years of Process/Manufacturing Engineering experience
  • Hands‑on experience with laser welding, resistance welding, battery/capacitor manufacturing, or related thermal joining technologies.
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